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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 496942Erstellt: 25. Oktober 2026

4'-Bromoacetanilide → N-Acetyl-4-aminobiphenyl

https://huagongshe.com/reaction/496942

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4'-BromoacetanilideHCID 7683—
EduktPhenylboronic AcidHCID 66827—
EduktPotassium FluorideHCID 522689—
Katalysatorpalladium(II) acetateHCID 167845—
Katalysator2-(Di-tert-butylphosphino)biphenylHCID 2734215—
ProduktN-Acetyl-4-aminobiphenylHCID 1999886,2%

Reaktionsschritte

An oven dried resealable Schlenk tube was evacuated and backfilled with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 1.0 mol %), 2-(di-tert-butylphosphino)biphenyl (6.0 mg, 0.02 mmol, 2.0 mol %), phenylboronic acid (183 mg, 1.5 mmol), potassium fluoride (174 mg, 3.0 mmol), and 4′-bromoacetanilide (214 mg, 1.0 mmol). The tube was evacuated and backfilled with argon, and THF (1 mL) was added through a rubber septum. The tube was sealed with a teflon screwcap, and the reaction mixture was stirred at room temperature until the starting aryl bromide had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ether (30 mL), filtered through celite, and concentrated. The crude material was purified by flash chromatography on silica gel to afford 182 mg (86%) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06946560B2
Quelldatensatzuspto-grants-2005_09
ORD IDord-8348f432382b4fea94f28602a0cba331
Quellennotizuspto-grants-2005_09